Next generation human skin constructs as advanced tools for drug development
Open accessAbstract
Many diseases, as well as side effects of drugs, manifest themselves through skin symptoms. Skin is a complex tissue that hosts various specialized cell types and performs many roles including physical barrier, immune and sensory functions. Therefore, modeling skin in vitro presents technical challenges for tissue engineering. Since the first attempts at engineering human epidermis in 1970s, there has been a growing interest in generating full-thickness skin constructs mimicking physiological functions by incorporating various skin components, such as vasculature and melanocytes for pigmentation. Development of biomimetic in vitro human skin models with these physiological functions provides a new tool for drug discovery, disease modeling, regenerative medicine and basic research for skin biology. This goal, however, has long been delayed by the limited availability of different cell types, the challenges in establishing co-culture conditions, and the ability to recapitulate the 3D anatomy of the skin. Recent breakthroughs in induced pluripotent stem cell (iPSC) technology and microfabrication techniques such as 3D-printing have allowed for building more reliable and complex in vitro skin models for pharmaceutical screening. In this review, we focus on the current developments and prevailing challenges in generating skin constructs with vasculature, skin appendages such as hair follicles, pigmentation, immune response, innervation, and hypodermis. Furthermore, we discuss the…
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PSOs offer a comprehensive physiological complexity compared to the previous 3D reconstructed skin models, representing a wide range of skin cell types, including melanocytes, neurons, adipocytes and Merkel cells.
“PSOs offer a comprehensive physiological complexity compared to the previous 3D reconstructed skin models [6], representing a wide range of skin cell types, including melanocytes, neurons, adipocytes and Merkel cells.”
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References 125 · Cited by 104
- Authors
- Abaci, H., Guo, Z., Doucet, Y., Jacków, J., & Christiano, A.
- Affiliations
- Columbia University Irving Medical Center (US)
- Department of Dermatology, Columbia University Medical Center, New York, NY 10032, USA
- Corresponding author
- Christiano, Angela
- Venue
- Experimental Biology and Medicine
- Publisher
- Frontiers Media SA
- Published
- 2017-06-07
- Volume
- 242
- Issue
- 17
- Pages
- 1657-1668
- ISSN
- 0071-3384 (ISSN-L)
- 1535-3702
- 1535-3699
- PMC
- PMC5786367
- OpenAlex
- W2622369378
- Cited by
- 104
- References
- 125
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 10 · 2023: 9 · 2022: 11 · 2021: 15 · 2020: 15 · 2019: 13 · 2018: 13 · 2017: 4
- FWCI
- 5.54
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Experimental Biology and Medicine (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research Portal (King's College London) (submittedVersion, other-oa)
- Funders
- National Center for Advancing Translational Sciences (3UH3EB017103-04S2)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Keywords
- in vitro skin model, induced pluripotent stem cells, drug screening, epidermolysis bullosa, psoriasis, organ-on-a-chip, skin vasculature, hair follicle, melanocytes, skin pigmentation, skin innervation, subcutaneous tissue, co-culture, high-throughput drug screening
- MeSH terms
- Humans, Skin, Skin Diseases, Tissue Engineering, Microfluidics, Regenerative Medicine, Microchip Analytical Procedures, Drug Discovery, Lab-On-A-Chip Devices, Induced Pluripotent Stem Cells
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